NM_001385641.1(SAMD11):c.2483G>C (p.Gly828Ala) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 19, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000961855.5
Allele description
NM_001385641.1(SAMD11):c.2483G>C (p.Gly828Ala)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Aug 23, 2022